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Clinical Trials/NCT02404246
NCT02404246
Completed
Not Applicable

Pilot Trial of Peer Support for Bipolar Disorder

Kaiser Permanente1 site in 1 country88 target enrollmentDecember 2005

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bipolar Disorder
Sponsor
Kaiser Permanente
Enrollment
88
Locations
1
Primary Endpoint
Mean differences in depression scores using the Structured Clinical Interview for DSM Disorders (SCID) for current depression and LIFE measure and timeline for depression
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This pilot effectiveness trial will evaluate the feasibility, acceptability, and effectiveness of a structured peer support program based on the Certified Peer Specialist Program of the Depression and Bipolar Support Alliance (DBSA).

Detailed Description

Bipolar disorder is a chronic and often disabling illness affecting 1-2% of US adults. Peer support programs are an innovative and promising model to reverse demoralization, activate consumers to seek more effective care, develop consumers' self-management skills, and restore participation in work and other social roles. Peer-led programs can address key barriers to dissemination of effective psychosocial treatment. This pilot effectiveness trial will evaluate the feasibility, acceptability, and effectiveness of a structured peer support program based on the Certified Peer Specialist Program of the Depression and Bipolar Support Alliance (DBSA). Following the philosophy of recovery, the intervention focuses on: * Motivating consumers to develop an expectation of recovery * Encouraging regular self-monitoring of mood symptoms * Training consumers to develop self-management skills for symptom control and problem solving * Activating consumers to be more informed partners in care and more effective self-advocates * Motivating and assisting consumers to reclaim work and other rewarding social roles The investigators will use a rigorous research design to evaluate how structured peer support promotes core values of mental health recovery. Impact of the intervention will be judged across a range of outcomes: * Long-term control of mood disorder symptoms * Optimal participation in work and other rewarding social roles * Consumers' perceptions of autonomy and full participation in the treatment process Findings from this pilot study will inform the development of a full-scale effectiveness trial to include a broader range of participants and health care settings.

Registry
clinicaltrials.gov
Start Date
December 2005
End Date
September 2009
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • GHC members aged 18 and over with Bipolar Disorder Type 1 or Type 2 and at least 6 weeks during the past 3 months with a depression or mania/hypomania Psychiatric Status Rating of 3 or greater (indicating significant symptoms at least half of the time). Potential participants will not be excluded because of medical, psychiatric, or substance use comorbidity.

Exclusion Criteria

  • Children under age 18.

Outcomes

Primary Outcomes

Mean differences in depression scores using the Structured Clinical Interview for DSM Disorders (SCID) for current depression and LIFE measure and timeline for depression

Time Frame: up to 9 months

Mania PSR scores using the Structured Clinical Interview for DSM Disorders (SCID) for mania/Hypo-mania and LIFE measure and timeline for mania

Time Frame: up to 9 months

Intervention program effects on consumer's perceptions of care across follow-ups using self-efficacy tool, POPP Empowerment ("Well-Being Module") and Health Care Climate questionnaire

Time Frame: up to 9 months

Secondary Outcomes

  • Mean number of weeks using mania PSR scores during follow-ups.(up to 9 months)
  • Mean number of weeks with depression during follow-ups.(up to 9 months)

Study Sites (1)

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